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HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT

K933722 Class I Traditional
Decision Date
1996-06-13
Sponsor / Applicant
Horizon Diagnostics, Inc.

Technical Specification

510(k) Submission ID K933722
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1996-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT received FDA 510(k) clearance under submission number K933722, sponsored by Horizon Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1996-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code CDT and 21 CFR 862.1705, within the Clinical Chemistry review panel as a Class I device.